Functional dichotomy of ribosomal proteins during the synthesis of mammalian 40S ribosomal subunits. - sprookjes - yvandenbroek - TriplyDB

Functional dichotomy of ribosomal proteins during the synthesis of mammalian 40S ribosomal subunits.

Functional dichotomy of ribosomal proteins during the synthesis of mammalian 40S ribosomal subunits.

http://www.wikidata.org/entity/Q34110999

about

Paradigms of ribosome synthesis: Lessons learned from ribosomal proteins RNA mimicry by the fap7 adenylate kinase in ribosome biogenesis Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypes The evolutionarily conserved protein Las1 is required for pre-rRNA processing at both ends of ITS2 Yeast polypeptide exit tunnel ribosomal proteins L17, L35 and L37 are necessary to recruit late-assembling factors required for 27SB pre-rRNA processing.Ribosomal proteins L7 and L8 function in concert with six A₃ assembly factors to propagate assembly of domains I and II of 25S rRNA in yeast 60S ribosomal subunits Role of ribosomal protein mutations in tumor development (Review)Gradual processing of the ITS1 from the nucleolus to the cytoplasm during synthesis of the human 18S rRNA Nuclear LC3 Associates with Slowly Diffusing Complexes that Survey the Nucleolus Two orthogonal cleavages separate subunit RNAs in mouse ribosome biogenesis Notchless-dependent ribosome synthesis is required for the maintenance of adult hematopoietic stem cells Proteomic Analysis of Liver Proteins in a Rat Model of Chronic Restraint Stress-Induced Depression A Ribosomopathy Reveals Decoding Defective Ribosomes Driving Human Dysmorphism Prioritizing genes for X-linked diseases using population exome data.Poly(A)-specific ribonuclease is a nuclear ribosome biogenesis factor involved in human 18S rRNA maturation.Whole-exome sequencing and functional studies identify RPS29 as a novel gene mutated in multicase Diamond-Blackfan anemia families.The human nucleolar protein FTSJ3 associates with NIP7 and functions in pre-rRNA processing Germline mutation of RPS20, encoding a ribosomal protein, causes predisposition to hereditary nonpolyposis colorectal carcinoma without DNA mismatch repair deficiency Interrelationships between yeast ribosomal protein assembly events and transient ribosome biogenesis factors interactions in early pre-ribosomes Ribosomal protein SA haploinsufficiency in humans with isolated congenital asplenia The emerging importance of ribosomal dysfunction in the pathogenesis of hematologic disorders.Ribosomal proteins and human diseases: pathogenesis, molecular mechanisms, and therapeutic implications Analysis of two human pre-ribosomal factors, bystin and hTsr1, highlights differences in evolution of ribosome biogenesis between yeast and mammals.Involvement of human ribosomal proteins in nucleolar structure and p53-dependent nucleolar stress Elucidation of motifs in ribosomal protein S9 that mediate its nucleolar localization and binding to NPM1/nucleophosmin Loss of nucleolar histone chaperone NPM1 triggers rearrangement of heterochromatin and synergizes with a deficiency in DNA methyltransferase DNMT3A to drive ribosomal DNA transcription.Identification and Expression Analysis of Ribosome Biogenesis Factor Co-orthologs in Solanum lycopersicum.An overview of pre-ribosomal RNA processing in eukaryotes Ribosomal protein gene deletions in Diamond-Blackfan anemia.Reduced expression of the mouse ribosomal protein Rpl17 alters the diversity of mature ribosomes by enhancing production of shortened 5.8S rRNA.Determinants of mammalian nucleolar architecture.Frameshift mutation in p53 regulator RPL26 is associated with multiple physical abnormalities and a specific pre-ribosomal RNA processing defect in diamond-blackfan anemia Mammalian HCA66 protein is required for both ribosome synthesis and centriole duplication hUTP24 is essential for processing of the human rRNA precursor at site A1, but not at site A0 Longevity GWAS Using the Drosophila Genetic Reference Panel.Ribosome biogenesis dysfunction leads to p53-mediated apoptosis and goblet cell differentiation of mouse intestinal stem/progenitor cells Comprehensive proteomic analysis of nonintegrin laminin receptor interacting proteins Functions of ribosomal proteins in assembly of eukaryotic ribosomes in vivo.Structure of a human pre-40S particle points to a role for RACK1 in the final steps of 18S rRNA processing.Human PDCD2L Is an Export Substrate of CRM1 That Associates with 40S Ribosomal Subunit Precursors.

P2860

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P2860

Functional dichotomy of ribosomal proteins during the synthesis of mammalian 40S ribosomal subunits.

http://www.wikidata.org/entity/Q34110999

description

2010 nî lūn-bûn

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2010 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Functional dichotomy of riboso ...... malian 40S ribosomal subunits.

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Functional dichotomy of riboso ...... malian 40S ribosomal subunits.

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Functional dichotomy of riboso ...... malian 40S ribosomal subunits.

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type

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Functional dichotomy of riboso ...... malian 40S ribosomal subunits.

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Functional dichotomy of riboso ...... malian 40S ribosomal subunits.

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Functional dichotomy of riboso ...... malian 40S ribosomal subunits.

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Functional dichotomy of riboso ...... malian 40S ribosomal subunits.

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Functional dichotomy of riboso ...... malian 40S ribosomal subunits.

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Functional dichotomy of riboso ...... malian 40S ribosomal subunits.

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Journal of Cell Biology

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Functional dichotomy of riboso ...... malian 40S ribosomal subunits.

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Gwennaële Fichant

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Marie-Françoise O'Donohue

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Marlène Faubladier

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Pierre-Emmanuel Gleizes

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Valérie Choesmel

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P2860

Ribosomal protein S27-like, a p53-inducible modulator of cell fate in response to genotoxic stress

Human RPS19, the gene mutated in Diamond-Blackfan anemia, encodes a ribosomal protein required for the maturation of 40S ribosomal subunits

Identification of RPS14 as a 5q- syndrome gene by RNA interference screen

Impaired ribosome biogenesis in Diamond-Blackfan anemia

Ribosomal protein S27L is a direct p53 target that regulates apoptosis

Mutation of ribosomal protein RPS24 in Diamond-Blackfan anemia results in a ribosome biogenesis disorder

Nuclear export and cytoplasmic processing of precursors to the 40S ribosomal subunits in mammalian cells.

A map of 75 human ribosomal protein genes

Ribosomal protein S17 gene (RPS17) is mutated in Diamond-Blackfan anemia

The role of human ribosomal proteins in the maturation of rRNA and ribosome production

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853-866

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scholarly article

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10.1083/JCB.201005117

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5

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190

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2010-09-01T00:00:00Z

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46158360

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20819938

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2935573

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